| Literature DB >> 19155028 |
Xiaonan Xie1, Kaori Yoneyama, Yuta Harada, Norio Fusegi, Yoichi Yamada, Satoshi Ito, Takao Yokota, Yasutomo Takeuchi, Koichi Yoneyama.
Abstract
A germination stimulant, fabacyl acetate, was purified from root exudates of pea (Pisum sativum L.) and its structure was determined as ent-2'-epi-4a,8a-epoxyorobanchyl acetate [(3aR,4R,4aR,8bS,E)-4a,8a-epoxy-8,8-dimethyl-3-(((R)-4-methyl-5-oxo-2,5-dihydrofuran-2-yloxy)methylene)-2-oxo-3,3a,4,5,6,7,8,8b-decahydro-2H-indeno[1,2-b]furan-4-yl acetate], by 1D and 2D NMR spectroscopic, ESI- and EI-MS spectrometric, X-ray crystallographic analyses, and by comparing the (1)H NMR spectroscopic data and relative retention times (RR(t)) in LC-MS and GC-MS with those of synthetic standards prepared from (+)-orobanchol and (+)-2'-epiorobanchol. The (1)H NMR spectroscopic data and RR(t) of fabacyl acetate were identical with those of an isomer prepared from (+)-2'-epiorobanchol except for the opposite sign in CD spectra. This is the first natural ent-strigolactone containing an epoxide group. Fabacyl acetate was previously detected in root exudates of other Fabaceae plants including faba bean (Vicia faba L.) and alfalfa (Medicago sativa L.).Entities:
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Year: 2009 PMID: 19155028 DOI: 10.1016/j.phytochem.2008.12.013
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072